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NEOSOFT UMBILICAL VESSEL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883866
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
69 days

NEOSOFT UMBILICAL VESSEL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K883866
510(k) Type
Traditional
Applicant
MENLO CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/1988
Days to Decision
69 days